Canonical Allele Identifier: CA307787689

Gene: TYROBP

Linked Data

• ClinVar Variation Id: 1214384
• ClinVar RCV Id: RCV001582118
• dbSNP Id: rs118043958
• gnomAD v2: 19-36398561-A-G
• gnomAD v3: 19-35907659-A-G
• gnomAD v4: 19-35907659-A-G
• MyVariant Identifiers: chr19:g.36398561A>G (hg19) ; chr19:g.35907659A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35907659A>G , CM000681.2:g.35907659A>G	GRCh38
NC_000019.9:g.36398561A>G , CM000681.1:g.36398561A>G	GRCh37
NC_000019.8:g.41090401A>G	NCBI36
NG_009304.1:g.5626T>C , LRG_607:g.5626T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.94+71T>C MANE Select	ENSP00000262629.3:n.94+71T>C
ENST00000262629.8:c.94+71T>C	ENSP00000262629.3:n.94+71T>C
ENST00000424586.7:c.62-79T>C	ENSP00000402371.3:n.62-79T>C
ENST00000544690.6:c.62-79T>C	ENSP00000445332.1:n.62-79T>C
ENST00000585626.1:n.161+71T>C
ENST00000585901.6:c.94+71T>C	ENSP00000468608.1:n.94+71T>C
ENST00000586946.1:c.87+71T>C	ENSP00000465656.1:n.87+71T>C
ENST00000587837.5:c.87+71T>C	ENSP00000465081.1:n.87+71T>C
ENST00000588439.1:n.160T>C
ENST00000589517.1:c.94+71T>C	ENSP00000468447.1:n.94+71T>C
NM_001173514.1:c.62-79T>C	NP_001166985.1:n.62-79T>C
NM_001173515.1:c.62-79T>C	NP_001166986.1:n.62-79T>C
NM_003332.3:c.94+71T>C , LRG_607t1:c.94+71T>C	NP_003323.1:n.94+71T>C
NM_198125.2:c.94+71T>C	NP_937758.1:n.94+71T>C
NR_033390.1:n.136-79T>C
NM_001173514.2:c.62-79T>C	NP_001166985.1:n.62-79T>C
NM_001173515.2:c.62-79T>C	NP_001166986.1:n.62-79T>C
NM_003332.4:c.94+71T>C MANE Select	NP_003323.1:n.94+71T>C
NM_198125.3:c.94+71T>C	NP_937758.1:n.94+71T>C
NR_033390.2:n.122-79T>C